Runx3 (GeneID: 156726) | Rattus norvegicus
Description: runt-related transcription factor 3 [Source:RGD Symbol;Acc:620082]
Synonyms:
Other ID(s): ENSRNOG00000054217
Protein Accession Numbers: NP_569109
Statistics: ClinVar(4) gnomAD(814) COSMIC(532)
ClinVar Pathogenicity of Variations help

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000308873 ENST00000338888 You are here now! ENST00000399916 You are here now! ENST00000540420 NP_001026850 You are here now! NP_001307601 You are here now! NP_004341


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
NO DOMAINS EXIST

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Adenocarcinoma Neoplasms ; 0.494 0.69
Celiac Disease Digestive System Diseases ; Nutritional and Metabolic Diseases ; 0.494 0.69
Esophageal Neoplasms Neoplasms ; Digestive System Diseases ; 0.494 0.69
Glioblastoma Neoplasms ; 0.494 0.69
Leukemia, Myelocytic, Acute Neoplasms ; 0.494 0.69
Lung Neoplasms Neoplasms ; Respiratory Tract Diseases ; 0.494 0.69
Malignant neoplasm of stomach Neoplasms ; Digestive System Diseases ; 0.494 0.69
Acute Myeloid Leukemia, M1 Neoplasms ; 0.494 0.69
Pustulosis of Palms and Soles Skin and Connective Tissue Diseases ; 0.494 0.69
Polycystic Ovary Syndrome Neoplasms ; Female Urogenital Diseases and Pregnancy Complications ; Endocrine System Diseases ; 0.494 0.69
Psoriasis Skin and Connective Tissue Diseases ; 0.494 0.69
Ankylosing spondylitis Musculoskeletal Diseases ; 0.494 0.69
Stomach Neoplasms Neoplasms ; Digestive System Diseases ; 0.494 0.69
Adenocarcinoma, Basal Cell Neoplasms ; 0.494 0.69
Adenocarcinoma, Oxyphilic Neoplasms ; 0.494 0.69
Carcinoma, Cribriform Neoplasms ; 0.494 0.69
Carcinoma, Granular Cell Neoplasms ; 0.494 0.69
Adenocarcinoma, Tubular Neoplasms ; 0.494 0.69
Malignant neoplasm of lung Neoplasms ; Respiratory Tract Diseases ; 0.494 0.69
Giant Cell Glioblastoma Neoplasms ; 0.494 0.69
Malignant neoplasm of esophagus Neoplasms ; Digestive System Diseases ; 0.494 0.69
Sclerocystic Ovaries Neoplasms ; Female Urogenital Diseases and Pregnancy Complications ; Endocrine System Diseases ; 0.494 0.69
Glioblastoma Multiforme Neoplasms ; 0.494 0.69
Hereditary Diffuse Gastric Cancer Neoplasms ; Digestive System Diseases ; 0.494 0.69
Acute Myeloid Leukemia (AML-M2) Neoplasms ; 0.494 0.69
Liver carcinoma Neoplasms ; Digestive System Diseases ; 0.494 0.69
NO RESULT FOUND
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